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http://hub.abes.fr/edp/periodical/jbio/2012/volume_205/issue_4/jbio2011021/authorship/3
http://hub.abes.fr/oup/periodical/humrep/2010/volume_25/issue_1/101093humrepdep355/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_23/101093hmgddi383/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_20/101093hmgddn209/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_17/101093hmgddp273/authorship/6
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_4/101093hmgddn389/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_13/101093hmgddn100/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_15/101093hmg10151591/authorship/26
http://hub.abes.fr/oup/periodical/hmg/2007/volume_17/issue_7/101093hmgddm373/authorship/7
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http://hub.abes.fr/edp/periodical/jbio/2012/volume_205/issue_4/jbio2011021/w
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles
FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development
Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems
Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation
Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutations
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
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